105676-33-3

Upstream product

• 105676-47-9 (2S,3R)-3-<(4S)-2,2-dimethyl-1,3-dioxolan-4-yl>-1,2-butanediol 
• 105676-49-1 1,2-anhydro-3-deoxy-3-C-methyl-4,5-O-isopropylidene-D-arabinitol 
• 105676-53-7 (3R,4R,5R)-5-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-3-methyl-hexane-1,4-diol 
• 105676-51-5 2,3,5-trideoxy-5-C-methyl-6,7-O-isopropylidene-D-arabino-hept-2-eno-1,4-lactone 
• 105676-52-6 2,3,5-trideoxy-3,5-di-C-methyl-D-talo-heptono-1,4-lactone 
• 105676-50-4 (R)-5-[(R)-1-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-ethyl]-3-phenylsulfanyl-dihydro-furan-2-one 
• 115495-43-7 (4R,5R)-5-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-4-hydroxy-2-phenylsulfanyl-hexanoic acid 
• 32780-06-6 (5S)-5-(hydroxymethyl)-2-oxo-tetrahydrofuran 
• 105676-46-8 (4S,5S)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-3-hydroxy-4-methyldihydrofuran-2(3H)-one 
• 105676-32-2 (S)-5-[(1R,3S)-5-(tert-Butyl-diphenyl-silanyloxy)-1,3-dimethyl-pentyl]-5H-furan-2-one 
• 5336-08-3 D-Ribono-1,4-lactone 
• 92512-33-9 (3R,4S,5R)-5-((tert-butyldiphenylsilyloxy)methyl)-3,4-dihydroxydihydrofuran-2(3H)-one 
• 115479-71-5 (4R,5R,7S)-9-(tert-Butyl-diphenyl-silanyloxy)-4-hydroxy-5,7-dimethyl-2-phenylselanyl-nonanoic acid 
• 106731-86-6 (S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-3-phenylselanyl-dihydro-furan-2-one 

Downstream Products

• 105676-42-4 [(2R,3R,4R)-3-Benzyloxy-4-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-methyl-pentyloxy]-tert-butyl-diphenyl-silane 
• 105676-36-6 Methanesulfonic acid (1S,2R,4S)-6-(tert-butyl-diphenyl-silanyloxy)-2,4-dimethyl-1-((R)-1-methyl-3-trityloxy-propyl)-hexyl ester 
• 105676-35-5 (3R,4S,5R,7S)-9-(tert-Butyl-diphenyl-silanyloxy)-3,5,7-trimethyl-1-trityloxy-nonan-4-ol 
• 105676-37-7 (3R,5S,7S)-1,9-dihydroxy-3,5,7-trimethyl-9-O-tert-butyldiphenylsilyl-1-O-triphenylmethyl-nonane 
• 105676-34-4 (3R,4S,5R,7S)-1,4,9-trihydroxy-3,5,7-trimethyl-9-O-tert-butyldiphenylsilyl-nonane 

Relevant academic research and scientific papers

STEREOCHEMICAL CONTROL OF NATURE'S BIOSYNTHETIC PATHWAYS: A GENERAL STRATEGY FOR THE SYNTHESIS OF POLYPROPIONATE-DERIVED STRUCTURAL UNITS FROM A SINGLE CHIRAL PROGENITOR

A general strategy that permits the stereocontrolled construction of acyclic chains containing vicinal and/or alternating alkyl and hydroxy substituents is presented.Structural subunits of ionomycin were synthesized from a common chiral intermediate.